Senior Statistical Programmer

Warman O'Brien; Poland; Hybrid; PLN 270,000 - 330,000; Full time

Benefits offered by this job

Bonus

Remote or hybrid work

Job summary

Warman O'Brien is seeking a Senior Statistical Programmer I/II to join a leading CRO. Role offers remote or hybrid options in Poland, including Warsaw, with a competitive salary and bonus eligibility.

You will lead statistical programming activities, develop SDTM/ADaM datasets, support regulatory submissions, mentor junior programmers, and help shape programming standards within a high-performing team.

Qualifications

• 5+ years of experience in clinical trial statistical programming.
• Strong hands-on experience with SDTM, ADaM, CDISC.
• Experience working in a CRO or pharmaceutical environment.
• Leadership of workstreams and cross-functional teams.
• Excellent attention to detail and problem-solving.
• Knowledge of regulatory submission processes is a plus.

Responsibilities

• Leading statistical programming activities across clinical studies.
• Developing, programming, and reviewing SDTM and ADaM datasets.
• Programming and reviewing TLGs for CSRs, ISS and ISE.
• Performing CDISC and Pinnacle 21 checks.
• Preparing and reviewing define.xml, aCRFs, and related documentation.
• Supporting regulatory submissions.
• Improving processes, macros, and programming standards.
• Mentoring and guiding less experienced programmers.

Skills

5+ years clinical trial programming

Leadership / cross-functional

Attention to detail

CRO/pharma experience

SDTM/ADaM/CDISC

Education

Master's degree in Statistics/Biostatistics/Mathematics/CS

Job description

Senior Statistical Programmer I / II | Leading CRO | Remote or Hybrid (Warsaw) | Poland | circa 300,000 ZL | Bonus |

Join an established, fast-growing CRO that is expanding its statistical programming team across Europe. They are looking for Senior Statistical Programmers to join from anywhere in Poland, with fully remote or hybrid options available in Warsaw.

This organisation is recognised for delivering high-quality clinical work, building strong client partnerships, and offering a genuinely flexible working culture. As they continue their European growth, they are carefully building a team of top-tier Statistical Programmers, making this a rare opportunity to join a highly specialised, high-performing environment where your expertise is truly valued and impactful. You’ll work at the forefront of clinical research, contribute to meaningful studies, and accelerate your career within an expert-led team.

In this role, you’ll take on a senior, hands-on position in statistical programming, leading projects, driving regulatory submissions, and ensuring high standards across deliverables. You’ll also play a key role in mentoring junior programmers and shaping best practices within the team.

Key responsibilities include:

• Leading statistical programming activities across clinical studies
• Developing, programming, and reviewing SDTM and ADaM datasets
• Programming and reviewing TLGs for CSRs, ISS and ISE
• Performing CDISC and Pinnacle 21 checks
• Preparing and reviewing define.xml, aCRFs, and related documentation
• Supporting regulatory submissions
• Improving processes, macros, and programming standards
• Mentoring and guiding less experienced programmers

What we’re looking for

• Masters degree in Statistics, Biostatistics, Mathematics, Computer Science, or similar
• 5+ years of experience in clinical trial statistical programming
• Strong hands-on experience with SDTM, ADaM, TLGs, and CDISC
• Experience working in a CRO or pharmaceutical environment
• Comfortable leading workstreams and collaborating with cross-functional teams
• High attention to detail, good organisation, and a practical approach to problem-solving

What’s on offer

• Remote or hybrid working in Poland
• Long-term role in a growing, independent CRO
• Exposure to varied studies and clients
• Supportive environment with room for professional development
• Generous salary, benefits and bonus